Journals / Perinatoloji Dergisi / 2021 / Cilt: 29 - Sayı: 3

Pregnancy onset congenital thrombotic thrombocytopenic purpura (Upshaw-Schulman syndrome) mimicking HELLP syndrome: a case report

HELLP sendromunu taklit eden gebelik başlangıçlı konjenital trombotik trombositopenik purpura (Upshaw-Schulman sendromu): Olgu sunumu

Pages
270–273
Publication Date
2022-10-18
DOI
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

We strive to have sufficient awareness in order to dis- tinguish these two pathologies from each other on an antenatal basis, because the causes of the managements are entirely different.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Objective: Thrombotic thrombocytopenic purpura is a thrombot- ic microangiopathic condition characterized by hemolytic anemia, thrombocytopenia, neurologic abnormalities, fever and renal dys- function.
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Key Findings & Data:In this report, we present a case at which we identified a novel mutation which led to a significant reduction of ADAMTS13 activity.
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Conclusion & Impact:We strive to have sufficient awareness in order to dis- tinguish these two pathologies from each other on an antenatal basis, because the causes of the managements are entirely different.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Objective: Thrombotic thrombocytopenic purpura is a thrombot- ic microangiopathic condition characterized by hemolytic anemia, thrombocytopenia, neurologic abnormalities, fever and renal dys- function. Thrombotic microangiopathies such as preeclampsia and HELLP syndrome are pregnancy-specific, whereas others such as thrombotic thrombocytopenic purpura (TTP) and hemolytic ure- mic syndrome are not. In this report, we present a case at which we identified a novel mutation which led to a significant reduction of ADAMTS13 activity. Case: A nulliparous pregnant woman of 32-year-old presenting with epigastric pain, hypertension and low platelet count was first sus- pected of HELLP syndrome, but was diagnosed with congenital TTP after delivery. Conclusion: HELLP syndrome co-existed with undiagnosed TTP in this case. We strive to have sufficient awareness in order to dis- tinguish these two pathologies from each other on an antenatal basis, because the causes of the managements are entirely different.

Özet

Amaç: Trombotik trombositopenik purpura; hemolitik anemi, trombositopeni, nörolojik anomaliler, atefl ve renal disfonksiyon ile karakterize trombotik mikroanjiyopatik bir hastal›kt›r. Preek- lampsi ve HELLP sendromu gibi trombotik mikroanjiyopatiler gebeli¤e özgüyken, trombotik trombositopenik purpura (TTP) ve hemolitik üremik sendrom gibi di¤er mikroanjiyopatiler gebeli¤e özgü de¤ildir. Bu raporda, ADAMTS13 aktivitesinde önemli bir azalmaya yol açan yeni bir mutasyon tespit etti¤imiz olgumuzu su- nuyoruz. Olgu: Epigastrik a¤r›, hipertansiyon ve düflük platelet say›s›yla baflvuran 32 yafl›ndaki nullipar gebede önce HELLP sendromun- dan flüphelenildi, fakat olguya do¤um sonras›nda konjenital TTP tan›s› ald›. Sonuç: Bu olguda tan› almam›fl TTP’nin yan› s›ra HELLP sendro- mu mevcuttu. ‹ki patolojiyi antenatal bir temelde birbirinden ay›rt edebilmek için yeterli fark›ndal›¤a sahip olmaya çal›flmaktay›z, çün- kü iki patolojinin yönetim nedenleri birbirinden tamamen farkl›d›r.

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Cite This Article

ÖZEL, A., CANBEK, S., KOBAL, B. B., ERGİN, B., YAZICI, Z., MUHCU, M., KAYA, A. H. (2022). Pregnancy onset congenital thrombotic thrombocytopenic purpura (Upshaw-Schulman syndrome) mimicking HELLP syndrome: a case report. Perinatoloji Dergisi, Cilt: 29 - Sayı: 3, 270–273. https://ajindex.com/articles/588319

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